CA2210711A1 - Transdermal formulation - Google Patents
Transdermal formulationInfo
- Publication number
- CA2210711A1 CA2210711A1 CA002210711A CA2210711A CA2210711A1 CA 2210711 A1 CA2210711 A1 CA 2210711A1 CA 002210711 A CA002210711 A CA 002210711A CA 2210711 A CA2210711 A CA 2210711A CA 2210711 A1 CA2210711 A1 CA 2210711A1
- Authority
- CA
- Canada
- Prior art keywords
- xanomeline
- transdermal
- formulation
- parts
- patch formulation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7038—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer
- A61K9/7046—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds
- A61K9/7053—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds, e.g. polyvinyl, polyisobutylene, polystyrene
- A61K9/7061—Polyacrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7084—Transdermal patches having a drug layer or reservoir, and one or more separate drug-free skin-adhesive layers, e.g. between drug reservoir and skin, or surrounding the drug reservoir; Liquid-filled reservoir patches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The present invention provides a method for treating Alzheimer's Disease using a xanomeline transdermal formation. The invention provides desired transdermal xanomeline patch formulations.
Description
CA 022l07ll l997-07-l6 W O 96/23463 PCTrUS~G/0~501 ~ A~) n~L~L FOFUrnI~TION
r The present invention provides a novel transdermal formulation containing the pharmaceutically active compound 3-[4-(hexyloxy)-1,2,5-thiadiazol-3-yl]-1,2,5,6-tetrahydro-1-methylpyridine (xanomeline).
Xanomeline, described in U.S. Patent No. 5,043,345 ('345), is a compound having muscarinic activity which can be useful for the treatment of Alzheimer's Disease. As set forth in the '345 patent, xanomeline can be prepared in a 15 solid form for oral use, in the form of suppositories for rectal administration, or in the form of sterile injectable solutions for parenteral use. A formulation for a typical tablet is provided; however, the patent does not suggest that it would be possible or desirable to prepare a transdermal 20 xanomeline patch formulation.
Applicants have discovered that the transdermal xanomeline patch formulation of this invention provides suprising beneficial effects. The present invention provides a method for treating Alzheimer's disease with fewer side 25 effects than are typically associated with muscarinic agonists like xanomeline.
The transdermal formulation of this invention provides consistent dosage of the active ingredient, achieves 30 sustained plasma concentration of the pharmaceutically active agent, and encourages patient compliance.
.
The present invention provides a transdermal xanomeline patch formulation comprising an effective amount of xanomeline, from 0.1 to 10 parts by weight azone, from 30 to 69.8 parts ethanol, 29 to 50 parts by weight water, from O
W 096/23463 PCT~US96/00504 to 30 parts by weight propylene glycol, and 1 to 5 parts by weight Klucel HF.
Further, there is provided a transdermal xanomeline patch formulation comprising an effective amount of xanomeline and from about 70 to 99.8~ acrylate adhesive.
There is provided a transdermal patch wherein xanomeline is intimately distributed in a matrix.
Additionally, there is provided a transdermal xanomeline patch formulation comprising an effective amount of xanomeline, from 85 to 97 parts by weight ethanol and from 2 to 14.9 parts Klucel HF.
Finally, there is provided a method for treating Alzheimer's disease comprising administering xanomeline transdermally using a patch formulation.
As used herein "xanomeline" shall refer to the free base, a pharmaceutically acceptable salt or solvate thereof.
The free base is preferred. The transdermal xanomeline patch formulations of the present invention provide surprising beneficial properties. The xanomeline tablet was associated with undesired parasympathomimetic effects when administered to humans. Applicants have discovered that the transdermal patch formulation can minimize such effects while providing higher sustained plasma levels of the pharmaceutically active agent.
Although the transdermal patch formulations claimed herein are preferred for the transdermal delivery of xanomeline, other transdermal formulations may be employed.
Percutaneous or transdermal delivery of pharmacologically active agents has become feasible in recent years largely due to vehicles therefor which allow increased permeation of said agents into the body surface to which applied. Such agents which may be useful for the preparation of a xanomeline transdermal patch formulation include, but are not necessarily limited to, dimethylsulfoxide (U.S. Patent No.
r The present invention provides a novel transdermal formulation containing the pharmaceutically active compound 3-[4-(hexyloxy)-1,2,5-thiadiazol-3-yl]-1,2,5,6-tetrahydro-1-methylpyridine (xanomeline).
Xanomeline, described in U.S. Patent No. 5,043,345 ('345), is a compound having muscarinic activity which can be useful for the treatment of Alzheimer's Disease. As set forth in the '345 patent, xanomeline can be prepared in a 15 solid form for oral use, in the form of suppositories for rectal administration, or in the form of sterile injectable solutions for parenteral use. A formulation for a typical tablet is provided; however, the patent does not suggest that it would be possible or desirable to prepare a transdermal 20 xanomeline patch formulation.
Applicants have discovered that the transdermal xanomeline patch formulation of this invention provides suprising beneficial effects. The present invention provides a method for treating Alzheimer's disease with fewer side 25 effects than are typically associated with muscarinic agonists like xanomeline.
The transdermal formulation of this invention provides consistent dosage of the active ingredient, achieves 30 sustained plasma concentration of the pharmaceutically active agent, and encourages patient compliance.
.
The present invention provides a transdermal xanomeline patch formulation comprising an effective amount of xanomeline, from 0.1 to 10 parts by weight azone, from 30 to 69.8 parts ethanol, 29 to 50 parts by weight water, from O
W 096/23463 PCT~US96/00504 to 30 parts by weight propylene glycol, and 1 to 5 parts by weight Klucel HF.
Further, there is provided a transdermal xanomeline patch formulation comprising an effective amount of xanomeline and from about 70 to 99.8~ acrylate adhesive.
There is provided a transdermal patch wherein xanomeline is intimately distributed in a matrix.
Additionally, there is provided a transdermal xanomeline patch formulation comprising an effective amount of xanomeline, from 85 to 97 parts by weight ethanol and from 2 to 14.9 parts Klucel HF.
Finally, there is provided a method for treating Alzheimer's disease comprising administering xanomeline transdermally using a patch formulation.
As used herein "xanomeline" shall refer to the free base, a pharmaceutically acceptable salt or solvate thereof.
The free base is preferred. The transdermal xanomeline patch formulations of the present invention provide surprising beneficial properties. The xanomeline tablet was associated with undesired parasympathomimetic effects when administered to humans. Applicants have discovered that the transdermal patch formulation can minimize such effects while providing higher sustained plasma levels of the pharmaceutically active agent.
Although the transdermal patch formulations claimed herein are preferred for the transdermal delivery of xanomeline, other transdermal formulations may be employed.
Percutaneous or transdermal delivery of pharmacologically active agents has become feasible in recent years largely due to vehicles therefor which allow increased permeation of said agents into the body surface to which applied. Such agents which may be useful for the preparation of a xanomeline transdermal patch formulation include, but are not necessarily limited to, dimethylsulfoxide (U.S. Patent No.
3,551,554); various 1-substituted azacycloalkan-2-ones such W O 96123463 PCTrUS96/00504 as azone (U.S. Patent Nos. 4,562,075, 4,405,616, 4,326,893 and 3,989,816); sugar esters in combination with sulfoxide or phosphine oxide (U.S. Patent Nos. 4,130,667, 4,130,643, 4,046,886, 3,952,099, and 3,896,238); lower alkyl amides (U.S. Patent No. 3,472,931); certain aliphatic sulfoxides (U.S. Patent No. 3,903,256); a composition containing glycerol monooleate, ethanol and isopropyl myristate (U.S.
Patent 4,335,115); a binary mixture of 1-dodecylazacycloheptan-2-one and a compound selected from a diol or a second N-substituted azacycloalkyl-2-one (U.S.
Patent Mo. 4,557,934); and polyethylene glycol monolaurate (U.S. Patent No. 4,568,343). U.S. Patent Nos. 3,551,554, 4,562,075, 4,405,616, 4,326,893, 3,989,816, 4,130,667, 4,130,643, 4,046,886, 3,952,099, 3,896,238, 3,472,931, 3,903,256, 4,335,115, 4,557,934, and 4,568 343 are hereby incorporated by reference in their entirety.
It is contemplated that the transdermal patch formulations of this invention will find utility in both humans and animals, i.e., will have both medical and veterinary applications for providing increased percutaneous absorption of the pharmaceutically active agent. As used herein, the term "percutaneous" refers to the passage of such agents through skin (typically intact).
The transdermal formulations of the present invention may be administered using a variety of devices which have been described in the art. For example, such devices include, but are not limited to those described in U.S. Patent Nos. 3,598,122, 3,598,123, 3,710,795, 3,731,683, 3,742,951, 3,814,097, 3,921,636, 3,972,995, 3,993,072, 3,993,073, 3,996,934, 4,031,894, 4,060,084, 4,069,307, 4,077,407, 4,201,211, 4,230,105, 4,292,299, and 4,292,303 each of which is hereby incorporated by reference in its entirety. The dosage forms of the present invention may incorporate certain pharmaceutically acceptable excipients - 35 which are conventional in the art. These include, but are CA 022l07ll l997-07-l6 W O 96123463 PCT~US9CJ0~'01 not limited to, gelling agents, cream and ointment bases, and the like.
Xanomeline shall be present in the claimed dosage forms in an effective amount. The term "an effective amount"
shall refer to an amount calculatecl to achieve and maintain blood levels which will bring about the desired beneficial or therapeutic effect over the period of time desired. These amounts will vary depending the amount of pharmacologically active agent required to achieve the desired beneficial or therapeutic effect, whether one or more patches will be administered simultaneously the specific formulation of the patch, the age and condition of the patient to be treated, and the like. Such conventional dosage titration techniques, familiar to the skilled artisan, may be utilized to determine the amount of xanomeline present in the ultimate pharmaceutical dosage form for any specific situation.
The pharmacologically active xanomeline is administered by known techniques such as placing the patch containing said agent and transdermal formulation therefor on a body surface and maintaining said source on said body surface in agent and composition transmitting relation thereto.
One of the transdermal xanomeline patch formulations utilizes ethanol, water, azone, and optionally propylene glycol to enhance the permeation of the pharmacologically active xanomeline. As noted supra., azone is known to be useful for transdermal permeation enhancement and is chemically l-dodecylazacyloheptan-2-one. Azone can be prepared as described in U.S. Patent No. 4,316,893, hereby incorporated by reference.
Formulation of the claimed compositions may be achieved by conventional methods, as by the simple mixing of all components thoroughly. The artisan will appreciate that compositions containing diols other than propylene glycol and alcohols other than ethanol (i.e., 2-propanol) may find utility in transdermal xanomeline compositions as a component :
W 096t23463 PCTAUS~5~00'04 of the formulation. To the extent that such formulation exhibits the characteristics of the present compositions, such formulations are considered to fall within the scope of the present invention.
The present invention provides a ~ransdermai xanomeline patch formulation comprising an effective amount of xanomeline, from 0.1 to 10 parts by weight azone, from 30 to 69.8 parts ethanol, 29 to 50 parts by weight water, from 0 to 30 parts by weight propylene glycol, and 1 to 5 parts by weight Klucel HF. Preferred ranges for the formulation include from 2 to 4 parts by weight azone, from 30 to 55 parts by weight ethanol, from 0 to 20 parts by weight propylene glycol, from 35 to 45 parts water, and from 2.5 to 3.5 parts Klucel HF. One preferred embodiment is to omit propylene glycol from the formulation.
There is provided a transdermal formulation patch wherein an effective amount of xanomeline is intimately distrubuted in a matrix. One such preferred matrix is a pressure sensitive adhesive.
Further, there is provided a transdermal xanomeline patch formulation comprising an effective amount of xanomeline and from about 50 to 99.9% by weight acrylic adhesive. A preferred range of acrylic adhesive comprises from about 65 to about 99.8~ by weight acrylic adhesive. A
further preferred range of acrylic adhesive comprises from about 70 to about 98% by weight acrylic adhesive. Another preferred range for the acrylate adhesive is from about 80 to 98 parts by weight. The acrylate adhesive is commercially available and may be purchased for example, from the National Starch and Chemical Corporation, Bridgewater, New Jersey 08807, catalog number 80-1054. The acrylate adhesive typically contains 48% solids in 33% ethyl acetate/28%
heptane/34~ isopropanol/5~ toluene by weight.
Additionally, there is provided a transdermal xanomeline patch formulation comprising an effective amount of xanomeline, from 85 to 97 parts by weight ethanol and from W 096/23463 PCTrUS~G/0~'01 2 to 14.9 parts Klucel HF. Klucel HF is a commercially available gelling agent. For example, Klucel HF may be purchased from Aqualon. Other appropriate gelling agents can be selected by the skilled artisan. Preferred ranges for the formulation are 92 to 96 parts by weight ethanol and 2.5 to 3.5 parts Klucel HF or other appropriate gelling agent.
Another preferred range for such formulations comprises from about 93 to about 95 parts by weight ethanol and from about 3 to about 3.5 parts gelling agent.
The compound xanomeline can be prepared as described in U.S. Patent No. 5,043,345 Sauerberg et. al.
('345) which is hereby incorporated by reference in its entirety. As disclosed in the '345 patent xanomeline can be use~ul for the treatment of Alzheimer's disease, severe painful conditions, glaucoma, and for the stimulation of cognitive function of the forebrain and hippocampus of mammals.
Xanomeline tablet formulation has been administered to mild and moderately severe Alzheimer's Disease patients.
Such tablet formulation of xanomeline was associated with undesired parasympathomimetic effects when administered to a group of subjects. Surprisingly, the presently claimed transdermal formulations of xanomeline can minimize or eliminate such effects while maintaining a consistent, desirable plasma concentration of the pharmacologically active agent.
This invention provides a method for treating a condition associated with modulation of a muscarinic receptor with m;nim~l or no parasympathomimetic effects comprising administering xanomeline transdermally. Examples of such conditions associated with modulation of a muscarinic receptor include, but are not in any way limited to decreased cognition, Alzheimer's Disease, and severe painful conditions. Preferred transdermal patch formulations include but are not limited to a patch formulation comprising an effective amount of xanomeline, azone, ethanol, water, =
optionally propylene glycol and Klucel HF; an effective amount of xanomeline intimately distributed in a matrix; an effective amount of xanomeline and an acrylic adhesive; an effective amount of xanomeline, ethanol, and Klucel HF;
described herein.
As reported herein, plasma levels were determined using gas chromatography methods familiar to the skilled artisan. The artisan can establish the appropriate conditions for the gas chromatographic analysis; however, one set of suggested conditions include the following:
A 30cm ~.25 ~um capillary column (J & W Scientific for example); hydrogen flow rate of 3.2 ml/min, helium flow rate of 14.3 ml/min, and air flow of 115.0 ml/min. The gradient column temperature is suggested to be 90 to 270~ C, detector at 250~C, and injector at 250~C. A suggested detection type is nitrogen-phosphorus. The artisan will recognize that other conditions will be effective as well;
however, the present conditions are provided as guidance to assist the artisan in choosing the most desired parameters for the present conditions.
Suitable enhancers may be additionally be alcohols like 1,2 propane diol, 1,3 butylene glycol, l-hexadecanol, 2-hydroxy fatty alcohols, 2-octyldodecanol, 2-propanol, benzyl alcohol, cetylstearyl alcohol, diethylene glycol, dipropylene glycol, dodecanol, ethanol, glycerol, hexanediol, octanol, oleyl alcohol, panthenol, phenylcthanol, polyethylene glycols, or polypropylene glycols, or fatty acids like capric acid, linoleic acid, lauric acid, myristic acid, n-valerianic acid, pelargonic acid, also other physiologically acceptable low molecular acids like e.g. 3-phenylpropionic acid, acetic acid, adipic acid, benzoic acid, salicyclic acid or their skin compatible salts.
Similarly, sulphates and sulphonates of fatty acids, like sodium cetylstearyl sulphate sodium lauryl sulphate may be used advantageously. Esters of the formula [CH3(CH2)mCOO]nR, in which m is an integer from 8 to 16, W O 96/23463 PCTrUS5~'W504 preferably from 8 to 12; n is 1 or 2, preferably 1 and R is a lower alkyl (Cl to C3 residue but also compounds like 1.3 diacetin, capric/caprylic triglyceride, diisopropyl adipate, ethyl oleate, ethylene glycol (di-)stearate, ethylene glycol monostearate, glycerol hydroxystearate, glycerol monostearate, hydrogenated castor oil, oleic acid esters, triacetin, alsophthalate esters like diethyl phthalate or, di-(2-ethylhexyl)-phthalate may be added to the composition.
Other compounds with an advantageous action on the drug substance skin flow include sulfoxides, e.g. dimethyl sulfoxide or dodecylmethyl sulfoxide, amides like diethyl-m-toluamide, dimethyl formamide, fatty acid diethanolamide, N2N
dimethyl acetamide, amines like diethanolamine or triethanol amine, ethylene glycol derivatives like ethoxylated castor oil, oleylalcohol/PEG-5-ether, glycerol ethers with polyethylene glycol, diethylenglycol monomethylether, diethylenglycol monoethylether, terpenes and terpenoids like menthol, thymol, cineol, isobornyl acetate, limonene and finally further compounds not belonging to a specific chemical defined group but known to those skilled in the art to be used for that purpose, e.g. dimethicon, squalen, dimethyl isosorbide, lecithine, glycofurol, urea, N-methyl pyrrolidone.
Acrylic Copolymers Acrylic copolymers are understood to be more specifically copolymers prepared from esters of acrylic acid and methacrylic acid with Cl to Clg alcohols, dimethylaminoethanol or other suitable alcoholic components, vinyl acetate, vinyl pyrrolidone, styrene, butadiene, acryl nitrile or other suitable compounds with a vinyl group.
The following examples are provided to more fully illustrate the invention claimed herein. The examples are provided for illustrative purposes only and are not intended to limit the scope of the invention in any way.
W096/23463 PCT~S~6/00504 13xamDle 1 Transdermal formulation Free Base A 0.5 g sample of xanomeline free base was dissolved in 9.25 g of ethanol (200 proof). A 0.75 g sample of azone and a 5.0 g aliquot of propylene glycol were added to the ethanol mixture with stirring. A 10 g sample of water was added to the mixture. The mixture was a cloudy suspension. Finally, 0.75 g of Klucel was added to the mixture and stirred until the Klucel was dispersed. The mixture was allowed to stand for 24 hours. A 2.0 g sample of the formulation prepared as described herein was dispensed by syringe into a reservoir-type transdermal adhesive system.
Time Concentration in Dog hours post a~lication na/ml Plasma 1 2 3 Mean + SEM
O O O 0 0+0 3 19 11 10 10.7+ 6.0 6 27 ~6 16 19.7+ 4.5 9 26 17 15 19.3+ 4.2 12 16 13 14 14.3+ 1.1 12 10 12 11.3+ 0.8 24 7 8 10 8.3+ 1.1 28 6 8 9 7.7+ 1.1 32 4 7 8 6.3+ 1.5 48 3 6 8 5.7+ 1.8 54 0 4 5 3.0+ 1.8 72 0 0 0 0+ 0 ~xam~le 2 Transdermal Formulation without Polvethvlene Glvcol A 0.5 g sample of xanomeline free base was dissolved in 13.0 g of ethanol (200 proof). A 0.75 g sample of azone was added to the ethanol mixture with stirring. An 11.25 g sample of water was added to the mixture. The mixture was a clear solution. Finally, 0.75 g of Klucel was W O 96/23463 PCTrU$96/00504 added to the mixture and stirred until the Klucel was dispersed. The mixture was allowed to stand for 24 hours. A
2.0 g sample of the formulation prepared as described herein was dispensed by syringe into a reservoir-type transdermal adhesive system.
Time Concentration in Dog hours ~ost a~lication na/ml Plasma 1 2 3 Mean + SEM
0 ~ ~ ~ ~+~
3 19 12 4 11.7+ 5.3 6 24 17 6 15.7+ 6.4 9 18 11 4 11.0+ 4.9 12 12 9 5 8.7+ 2.5 9 8 3 6.7+ 2.3 24 6 5 3 4.7+ 1.1 28 9 ~ 0 4.3+ 3.2 32 7 3 0 3.3+ 2.5 48 3 0 3 2.0+ 1.2 54 0 0 0 0+ 0 72 0 0 0 0+ 0 Time Concentration in Mo~key hours post a~lication n~/ml Plasma 1 2 3 Mean + SEM
O O , O 0 0+0 3 50 59 65 58+ 5.3 6 44 50 59 51+ 5.3 8 39 45 45 43i 2.5 12 25 42 41 36+ 6.7 34 37 22+ 11.8 24 14 13 16 14.3+ 1.1 28 . 12 8 8 9.3+ 1.6 32 9 7 7 7.7+ 0.8 48 5 5 4 4.7+ 0.4 54 2 2 2 2+ 0 72 0 0 0 0+ 0 W O 96/23463 PCTrUS96/OOS04 Patches were applied to the shaved chest of each rhesus monkey.
ExamDle 3 Transdermal Xanomeline in Gel A 1.0 g sample of xanomeline free base was dissolved in 47.5 g of ethanol (200-proof). Then a 1.5 g sample of Klucel gelling agent was added to the solution and stirred until dispersed. The gel was allowed to stand for 24 hours. A 2.0 g sample of the formulation prepared as such was dispensed by syringe into a reservoir-type transdermal adhesive system.
The patches prepared as stated herein were applied to rats. The rats were killed in pairs at various time points after application and the rat brains were removed and frozen. The binding of the Ml antagonist ligand, 3H-pirenzepine, to muscarinic receptors in the brain was determined. The decrease in binding is indicative of drug or active metabolite present in the brain. The effect of the drug after oral administration lasts less than 6 hours.
The percent of control ex vivo pirenzepine binding at 6 hours was 33%, at 12 hours 15%, at 24 hours 26%, and at 48 hours 53%. The mean plasma concentration using this patch formulation was as follows:
30 Time Mean Plasma Concentration (ng/ml) + SEM
6 109.8 + 35.53 12 152.4 + 30.18 24 115.9 + 43.02 48 28.07 + 5.995 W096/23463 PCT~S5~/0050q ~xamPle 4 Transdermal Xanomeline in Acrvlic Adhesive A 600 mg sample of xanomeline free base was dissolved in 41.6 g of pressure sensitive acrylic adhesive (cat. number 80-1054, National Starch and Chemical Corporation, Bridgewater, New Jersey 08807). The mixture was agitated for 2 hours on a three roller mill. The mixture was coated along the length of a 3 mil thick release liner using a knife coater providing a 20 mil gap. The 20 mil gap provides an effective 20 mil thick coating of the formulation on the release liner. The sample was allowed to air dry for 24 hours. The sample was laminated on polyester backing.
The patches prepared as stated herein were applied to rats. The rats were killed in pairs at various time points after application and the rat brains were removed and frozen. The binding of the M1 antagonist ligand, 3H-pirenzepine, to muscarinic receptors in the brain was determined. The decrease in binding is indicative of drug or active metabolite present in the brain. The effect of the drug after oral administration lasts less than 6 hours.
The percent of control ex vivo pirenzepine binding at 6 hours was 101%, at 12 hours 89%, at 24 hours 75%, and at 48 hours 105%.
A transdermal xanomeline patch formulation in acrylic adhesive was prepared substantially as described supra; however, the patch formulation comprised 10.8 g xanomeline per m2 (18% by weight) and 60 g of acrylic adhesive per m2 (82% by weight). Individual 25 cm2 patches were prepared to provide 27.2 mg of xanomeline free base per patch. The patches were applied to the shaved abdomen of rats and the shaved chest of monkeys. The patches were removed at 24 hours.
W 096/23463 PCTrUS96/00504 Nean Plasma Concentration in Rat Time(n~/ml) + SEM N-1.004.635 + 1.750 3 2.007.198 + 0.986 3 4.0011.211 + 0.883 3 6.0010.398 + 1.251 3 8.008.261 + 1.193 3 10.009.576 + 0.000 15.0012.284 + 3.107 3 18.009.435 + 1.540 3 24.0010.870 + 0.319 3 30.000.522 + 0.268 3 Two such adhesive patches were applied to the shaved chest of each monkey. The patches were removed at 24 hours.
Nean Plasma Concentration in Monk~y Time(n~/ml) + SEM N
1.5025.750 + 2.160 3 3.0035.467 + 1.840 3 6.0031.070 + 2.352 3 9.0031.300 + 1.578 3 12.0030.230 + 3.413 3 24.0027.037 + 1.868 3 28.008.917 + 3.301 3 32.004.867 + 2.622 3 48.001.080 + 0.571 3 One such adhesive patch was applied to the chest of each monkey. The patches were removed at 24 hours.
CA 022l07ll l997-07-l6 W 096/23463 PCTrUS~G/C~'01 Mean Plasma Conce~tration in Mo~key Time (n~/ml) ~ SEM N
1.50 6.940 + 0.205 3 3.00 9.897 i 1.642 3 6.00 9.757 + 0.802 3 g oo 9.433 + 1.140 3 12.00 9.760 + 1.160 3 24.00 9.330 + 0.589 3 28.00 1.793 + 0.101 3 32.00 0.800 + 0.055 3 48.00 0.123 + 0.072 3 Exam~le 5 Trans~r~l Xanomeline in Acrvlic Adhesive 9.0g Xanomeline free base are dissolved in 91g of an acrylic adhesive solution (solids content 50.0%, cat. number 901-1052, National Starch & Chemical, Zutphen, The Metherlands).The mixture is stirred for at least 0.5 hours and is coated on a 4 mil siliconized polyethylene terephthalate release liner to provide a coated layer of 60 g/m2 (based on dried matter). The wet layer is dried for 30 minutes at room temperature, then for 10 minutes at 50 C. The sample was laminated on a l-mil-backing layer of polyetylene terephthalate.
Test samples of approximately 5 cm2 are punched for in vitro skin permeation experiments on pig ear full thickness skin (Franz type diffusion cell, at 37 C; phosphate buffer pH 4.4 as receptor fluid). A mean (n=3) cumulative permeated amount of 46 ~g Xanomeline was found after 24 hours.
W O 96/23463 PCT~US96/00504 ~XamDle 6 Transdermal Xanomeline in Ac~Ylic ~hecive 14.3g Xanomeline free base are dissolved in 85.7g of an acrylic adhesive solution (solids content 50.0%, cat. number 901-1052, National Starch & Chemical, Zutphen, The Netherlands).
The mixture is stirred for at least 0.5 hours and is coated on a 4 mil siliconized polyethylene terephthalate release liner to provide a coated layer of 60g/m2 (based on dried matter). The wet layer is dried for 30 minutes at room temperature, then for 10 minutes at 50~C. The sample was laminated on a 1-mil-backing layer of polyethylene terephthalate.
Test samples of approximately 5 cm2 are punched for in vitro skin permeation experiments on pig ear full thickness skin (Franz type diffusion cell, at 37~C; phosphate buffer pH 5.5 as receptor fluid). A mean (n=3) cumulative permeated amount of 102 ~g Xanomeline was found after 24 hours.
Exam~le 7 Trans~err-l ~An~m~line in AcrYlic Adhesive 18.0g Xanomeline free base are dissolved in 82g of an acrylic adhesive solution (solids content 50.0%, cat. number 901-1052, National Starch & Chemical, Zutphen, The Netherlands).
The mixture is stirred for at least 0.5 hours and is coated on a 4 mil siliconized polyethylene terephthalate release liner to provide a coated layer of 60 g/m2 (based on dried matter). The wet layer is dried for 30 minutes at room temperature, then for 10 minutes at 50 C. The sample was laminated on a 1-mil-backing layer of polymethacrylic copolymer.
CA 022l07ll l997-07-l6 W 096123463 PCTrUS96/00~04 Test samples of approximately 5 cm2 are punched for in vitro skin permeation experiments on pig ear full thickness skin (Franz type diffusion cell, at 37 C; phosphate buffer pH 5.5 as receptor fluid). A mean (n=2) cumulative permeated amount of 332 ,ug Xanomeline was found after 24 hours.
Examples 5 to 7 illustrate the dependence of xanomeline permeation rate on the concentration o~ the drug.
According to Fick's law, one would expect a linear increase in diffusion (and permeation ) rate with increasing drug concentration. However, the following results based on the examples show an unexpected increase.
Xanomeline Concentration in Permeated after 24 hours dry adhesive matrix (% w/w) ~g/cm2 18 46 (Example 5) 28. 5 102 (Example 6) 36 332 (Example 7) The values had been derived from clear solutions of the drug in the adhesive. Unfortunately, the saturation limit of about 23-28g6 (W/W) in this polymer limits the utilization of this unexpected advantage of highly enriched xanomeline preparations. It is concluded from this unexpected results that an optimum formulation has to contain a slightly subsaturated, saturated or even supersaturated amount of xanomeline for best performance.
Patent 4,335,115); a binary mixture of 1-dodecylazacycloheptan-2-one and a compound selected from a diol or a second N-substituted azacycloalkyl-2-one (U.S.
Patent Mo. 4,557,934); and polyethylene glycol monolaurate (U.S. Patent No. 4,568,343). U.S. Patent Nos. 3,551,554, 4,562,075, 4,405,616, 4,326,893, 3,989,816, 4,130,667, 4,130,643, 4,046,886, 3,952,099, 3,896,238, 3,472,931, 3,903,256, 4,335,115, 4,557,934, and 4,568 343 are hereby incorporated by reference in their entirety.
It is contemplated that the transdermal patch formulations of this invention will find utility in both humans and animals, i.e., will have both medical and veterinary applications for providing increased percutaneous absorption of the pharmaceutically active agent. As used herein, the term "percutaneous" refers to the passage of such agents through skin (typically intact).
The transdermal formulations of the present invention may be administered using a variety of devices which have been described in the art. For example, such devices include, but are not limited to those described in U.S. Patent Nos. 3,598,122, 3,598,123, 3,710,795, 3,731,683, 3,742,951, 3,814,097, 3,921,636, 3,972,995, 3,993,072, 3,993,073, 3,996,934, 4,031,894, 4,060,084, 4,069,307, 4,077,407, 4,201,211, 4,230,105, 4,292,299, and 4,292,303 each of which is hereby incorporated by reference in its entirety. The dosage forms of the present invention may incorporate certain pharmaceutically acceptable excipients - 35 which are conventional in the art. These include, but are CA 022l07ll l997-07-l6 W O 96123463 PCT~US9CJ0~'01 not limited to, gelling agents, cream and ointment bases, and the like.
Xanomeline shall be present in the claimed dosage forms in an effective amount. The term "an effective amount"
shall refer to an amount calculatecl to achieve and maintain blood levels which will bring about the desired beneficial or therapeutic effect over the period of time desired. These amounts will vary depending the amount of pharmacologically active agent required to achieve the desired beneficial or therapeutic effect, whether one or more patches will be administered simultaneously the specific formulation of the patch, the age and condition of the patient to be treated, and the like. Such conventional dosage titration techniques, familiar to the skilled artisan, may be utilized to determine the amount of xanomeline present in the ultimate pharmaceutical dosage form for any specific situation.
The pharmacologically active xanomeline is administered by known techniques such as placing the patch containing said agent and transdermal formulation therefor on a body surface and maintaining said source on said body surface in agent and composition transmitting relation thereto.
One of the transdermal xanomeline patch formulations utilizes ethanol, water, azone, and optionally propylene glycol to enhance the permeation of the pharmacologically active xanomeline. As noted supra., azone is known to be useful for transdermal permeation enhancement and is chemically l-dodecylazacyloheptan-2-one. Azone can be prepared as described in U.S. Patent No. 4,316,893, hereby incorporated by reference.
Formulation of the claimed compositions may be achieved by conventional methods, as by the simple mixing of all components thoroughly. The artisan will appreciate that compositions containing diols other than propylene glycol and alcohols other than ethanol (i.e., 2-propanol) may find utility in transdermal xanomeline compositions as a component :
W 096t23463 PCTAUS~5~00'04 of the formulation. To the extent that such formulation exhibits the characteristics of the present compositions, such formulations are considered to fall within the scope of the present invention.
The present invention provides a ~ransdermai xanomeline patch formulation comprising an effective amount of xanomeline, from 0.1 to 10 parts by weight azone, from 30 to 69.8 parts ethanol, 29 to 50 parts by weight water, from 0 to 30 parts by weight propylene glycol, and 1 to 5 parts by weight Klucel HF. Preferred ranges for the formulation include from 2 to 4 parts by weight azone, from 30 to 55 parts by weight ethanol, from 0 to 20 parts by weight propylene glycol, from 35 to 45 parts water, and from 2.5 to 3.5 parts Klucel HF. One preferred embodiment is to omit propylene glycol from the formulation.
There is provided a transdermal formulation patch wherein an effective amount of xanomeline is intimately distrubuted in a matrix. One such preferred matrix is a pressure sensitive adhesive.
Further, there is provided a transdermal xanomeline patch formulation comprising an effective amount of xanomeline and from about 50 to 99.9% by weight acrylic adhesive. A preferred range of acrylic adhesive comprises from about 65 to about 99.8~ by weight acrylic adhesive. A
further preferred range of acrylic adhesive comprises from about 70 to about 98% by weight acrylic adhesive. Another preferred range for the acrylate adhesive is from about 80 to 98 parts by weight. The acrylate adhesive is commercially available and may be purchased for example, from the National Starch and Chemical Corporation, Bridgewater, New Jersey 08807, catalog number 80-1054. The acrylate adhesive typically contains 48% solids in 33% ethyl acetate/28%
heptane/34~ isopropanol/5~ toluene by weight.
Additionally, there is provided a transdermal xanomeline patch formulation comprising an effective amount of xanomeline, from 85 to 97 parts by weight ethanol and from W 096/23463 PCTrUS~G/0~'01 2 to 14.9 parts Klucel HF. Klucel HF is a commercially available gelling agent. For example, Klucel HF may be purchased from Aqualon. Other appropriate gelling agents can be selected by the skilled artisan. Preferred ranges for the formulation are 92 to 96 parts by weight ethanol and 2.5 to 3.5 parts Klucel HF or other appropriate gelling agent.
Another preferred range for such formulations comprises from about 93 to about 95 parts by weight ethanol and from about 3 to about 3.5 parts gelling agent.
The compound xanomeline can be prepared as described in U.S. Patent No. 5,043,345 Sauerberg et. al.
('345) which is hereby incorporated by reference in its entirety. As disclosed in the '345 patent xanomeline can be use~ul for the treatment of Alzheimer's disease, severe painful conditions, glaucoma, and for the stimulation of cognitive function of the forebrain and hippocampus of mammals.
Xanomeline tablet formulation has been administered to mild and moderately severe Alzheimer's Disease patients.
Such tablet formulation of xanomeline was associated with undesired parasympathomimetic effects when administered to a group of subjects. Surprisingly, the presently claimed transdermal formulations of xanomeline can minimize or eliminate such effects while maintaining a consistent, desirable plasma concentration of the pharmacologically active agent.
This invention provides a method for treating a condition associated with modulation of a muscarinic receptor with m;nim~l or no parasympathomimetic effects comprising administering xanomeline transdermally. Examples of such conditions associated with modulation of a muscarinic receptor include, but are not in any way limited to decreased cognition, Alzheimer's Disease, and severe painful conditions. Preferred transdermal patch formulations include but are not limited to a patch formulation comprising an effective amount of xanomeline, azone, ethanol, water, =
optionally propylene glycol and Klucel HF; an effective amount of xanomeline intimately distributed in a matrix; an effective amount of xanomeline and an acrylic adhesive; an effective amount of xanomeline, ethanol, and Klucel HF;
described herein.
As reported herein, plasma levels were determined using gas chromatography methods familiar to the skilled artisan. The artisan can establish the appropriate conditions for the gas chromatographic analysis; however, one set of suggested conditions include the following:
A 30cm ~.25 ~um capillary column (J & W Scientific for example); hydrogen flow rate of 3.2 ml/min, helium flow rate of 14.3 ml/min, and air flow of 115.0 ml/min. The gradient column temperature is suggested to be 90 to 270~ C, detector at 250~C, and injector at 250~C. A suggested detection type is nitrogen-phosphorus. The artisan will recognize that other conditions will be effective as well;
however, the present conditions are provided as guidance to assist the artisan in choosing the most desired parameters for the present conditions.
Suitable enhancers may be additionally be alcohols like 1,2 propane diol, 1,3 butylene glycol, l-hexadecanol, 2-hydroxy fatty alcohols, 2-octyldodecanol, 2-propanol, benzyl alcohol, cetylstearyl alcohol, diethylene glycol, dipropylene glycol, dodecanol, ethanol, glycerol, hexanediol, octanol, oleyl alcohol, panthenol, phenylcthanol, polyethylene glycols, or polypropylene glycols, or fatty acids like capric acid, linoleic acid, lauric acid, myristic acid, n-valerianic acid, pelargonic acid, also other physiologically acceptable low molecular acids like e.g. 3-phenylpropionic acid, acetic acid, adipic acid, benzoic acid, salicyclic acid or their skin compatible salts.
Similarly, sulphates and sulphonates of fatty acids, like sodium cetylstearyl sulphate sodium lauryl sulphate may be used advantageously. Esters of the formula [CH3(CH2)mCOO]nR, in which m is an integer from 8 to 16, W O 96/23463 PCTrUS5~'W504 preferably from 8 to 12; n is 1 or 2, preferably 1 and R is a lower alkyl (Cl to C3 residue but also compounds like 1.3 diacetin, capric/caprylic triglyceride, diisopropyl adipate, ethyl oleate, ethylene glycol (di-)stearate, ethylene glycol monostearate, glycerol hydroxystearate, glycerol monostearate, hydrogenated castor oil, oleic acid esters, triacetin, alsophthalate esters like diethyl phthalate or, di-(2-ethylhexyl)-phthalate may be added to the composition.
Other compounds with an advantageous action on the drug substance skin flow include sulfoxides, e.g. dimethyl sulfoxide or dodecylmethyl sulfoxide, amides like diethyl-m-toluamide, dimethyl formamide, fatty acid diethanolamide, N2N
dimethyl acetamide, amines like diethanolamine or triethanol amine, ethylene glycol derivatives like ethoxylated castor oil, oleylalcohol/PEG-5-ether, glycerol ethers with polyethylene glycol, diethylenglycol monomethylether, diethylenglycol monoethylether, terpenes and terpenoids like menthol, thymol, cineol, isobornyl acetate, limonene and finally further compounds not belonging to a specific chemical defined group but known to those skilled in the art to be used for that purpose, e.g. dimethicon, squalen, dimethyl isosorbide, lecithine, glycofurol, urea, N-methyl pyrrolidone.
Acrylic Copolymers Acrylic copolymers are understood to be more specifically copolymers prepared from esters of acrylic acid and methacrylic acid with Cl to Clg alcohols, dimethylaminoethanol or other suitable alcoholic components, vinyl acetate, vinyl pyrrolidone, styrene, butadiene, acryl nitrile or other suitable compounds with a vinyl group.
The following examples are provided to more fully illustrate the invention claimed herein. The examples are provided for illustrative purposes only and are not intended to limit the scope of the invention in any way.
W096/23463 PCT~S~6/00504 13xamDle 1 Transdermal formulation Free Base A 0.5 g sample of xanomeline free base was dissolved in 9.25 g of ethanol (200 proof). A 0.75 g sample of azone and a 5.0 g aliquot of propylene glycol were added to the ethanol mixture with stirring. A 10 g sample of water was added to the mixture. The mixture was a cloudy suspension. Finally, 0.75 g of Klucel was added to the mixture and stirred until the Klucel was dispersed. The mixture was allowed to stand for 24 hours. A 2.0 g sample of the formulation prepared as described herein was dispensed by syringe into a reservoir-type transdermal adhesive system.
Time Concentration in Dog hours post a~lication na/ml Plasma 1 2 3 Mean + SEM
O O O 0 0+0 3 19 11 10 10.7+ 6.0 6 27 ~6 16 19.7+ 4.5 9 26 17 15 19.3+ 4.2 12 16 13 14 14.3+ 1.1 12 10 12 11.3+ 0.8 24 7 8 10 8.3+ 1.1 28 6 8 9 7.7+ 1.1 32 4 7 8 6.3+ 1.5 48 3 6 8 5.7+ 1.8 54 0 4 5 3.0+ 1.8 72 0 0 0 0+ 0 ~xam~le 2 Transdermal Formulation without Polvethvlene Glvcol A 0.5 g sample of xanomeline free base was dissolved in 13.0 g of ethanol (200 proof). A 0.75 g sample of azone was added to the ethanol mixture with stirring. An 11.25 g sample of water was added to the mixture. The mixture was a clear solution. Finally, 0.75 g of Klucel was W O 96/23463 PCTrU$96/00504 added to the mixture and stirred until the Klucel was dispersed. The mixture was allowed to stand for 24 hours. A
2.0 g sample of the formulation prepared as described herein was dispensed by syringe into a reservoir-type transdermal adhesive system.
Time Concentration in Dog hours ~ost a~lication na/ml Plasma 1 2 3 Mean + SEM
0 ~ ~ ~ ~+~
3 19 12 4 11.7+ 5.3 6 24 17 6 15.7+ 6.4 9 18 11 4 11.0+ 4.9 12 12 9 5 8.7+ 2.5 9 8 3 6.7+ 2.3 24 6 5 3 4.7+ 1.1 28 9 ~ 0 4.3+ 3.2 32 7 3 0 3.3+ 2.5 48 3 0 3 2.0+ 1.2 54 0 0 0 0+ 0 72 0 0 0 0+ 0 Time Concentration in Mo~key hours post a~lication n~/ml Plasma 1 2 3 Mean + SEM
O O , O 0 0+0 3 50 59 65 58+ 5.3 6 44 50 59 51+ 5.3 8 39 45 45 43i 2.5 12 25 42 41 36+ 6.7 34 37 22+ 11.8 24 14 13 16 14.3+ 1.1 28 . 12 8 8 9.3+ 1.6 32 9 7 7 7.7+ 0.8 48 5 5 4 4.7+ 0.4 54 2 2 2 2+ 0 72 0 0 0 0+ 0 W O 96/23463 PCTrUS96/OOS04 Patches were applied to the shaved chest of each rhesus monkey.
ExamDle 3 Transdermal Xanomeline in Gel A 1.0 g sample of xanomeline free base was dissolved in 47.5 g of ethanol (200-proof). Then a 1.5 g sample of Klucel gelling agent was added to the solution and stirred until dispersed. The gel was allowed to stand for 24 hours. A 2.0 g sample of the formulation prepared as such was dispensed by syringe into a reservoir-type transdermal adhesive system.
The patches prepared as stated herein were applied to rats. The rats were killed in pairs at various time points after application and the rat brains were removed and frozen. The binding of the Ml antagonist ligand, 3H-pirenzepine, to muscarinic receptors in the brain was determined. The decrease in binding is indicative of drug or active metabolite present in the brain. The effect of the drug after oral administration lasts less than 6 hours.
The percent of control ex vivo pirenzepine binding at 6 hours was 33%, at 12 hours 15%, at 24 hours 26%, and at 48 hours 53%. The mean plasma concentration using this patch formulation was as follows:
30 Time Mean Plasma Concentration (ng/ml) + SEM
6 109.8 + 35.53 12 152.4 + 30.18 24 115.9 + 43.02 48 28.07 + 5.995 W096/23463 PCT~S5~/0050q ~xamPle 4 Transdermal Xanomeline in Acrvlic Adhesive A 600 mg sample of xanomeline free base was dissolved in 41.6 g of pressure sensitive acrylic adhesive (cat. number 80-1054, National Starch and Chemical Corporation, Bridgewater, New Jersey 08807). The mixture was agitated for 2 hours on a three roller mill. The mixture was coated along the length of a 3 mil thick release liner using a knife coater providing a 20 mil gap. The 20 mil gap provides an effective 20 mil thick coating of the formulation on the release liner. The sample was allowed to air dry for 24 hours. The sample was laminated on polyester backing.
The patches prepared as stated herein were applied to rats. The rats were killed in pairs at various time points after application and the rat brains were removed and frozen. The binding of the M1 antagonist ligand, 3H-pirenzepine, to muscarinic receptors in the brain was determined. The decrease in binding is indicative of drug or active metabolite present in the brain. The effect of the drug after oral administration lasts less than 6 hours.
The percent of control ex vivo pirenzepine binding at 6 hours was 101%, at 12 hours 89%, at 24 hours 75%, and at 48 hours 105%.
A transdermal xanomeline patch formulation in acrylic adhesive was prepared substantially as described supra; however, the patch formulation comprised 10.8 g xanomeline per m2 (18% by weight) and 60 g of acrylic adhesive per m2 (82% by weight). Individual 25 cm2 patches were prepared to provide 27.2 mg of xanomeline free base per patch. The patches were applied to the shaved abdomen of rats and the shaved chest of monkeys. The patches were removed at 24 hours.
W 096/23463 PCTrUS96/00504 Nean Plasma Concentration in Rat Time(n~/ml) + SEM N-1.004.635 + 1.750 3 2.007.198 + 0.986 3 4.0011.211 + 0.883 3 6.0010.398 + 1.251 3 8.008.261 + 1.193 3 10.009.576 + 0.000 15.0012.284 + 3.107 3 18.009.435 + 1.540 3 24.0010.870 + 0.319 3 30.000.522 + 0.268 3 Two such adhesive patches were applied to the shaved chest of each monkey. The patches were removed at 24 hours.
Nean Plasma Concentration in Monk~y Time(n~/ml) + SEM N
1.5025.750 + 2.160 3 3.0035.467 + 1.840 3 6.0031.070 + 2.352 3 9.0031.300 + 1.578 3 12.0030.230 + 3.413 3 24.0027.037 + 1.868 3 28.008.917 + 3.301 3 32.004.867 + 2.622 3 48.001.080 + 0.571 3 One such adhesive patch was applied to the chest of each monkey. The patches were removed at 24 hours.
CA 022l07ll l997-07-l6 W 096/23463 PCTrUS~G/C~'01 Mean Plasma Conce~tration in Mo~key Time (n~/ml) ~ SEM N
1.50 6.940 + 0.205 3 3.00 9.897 i 1.642 3 6.00 9.757 + 0.802 3 g oo 9.433 + 1.140 3 12.00 9.760 + 1.160 3 24.00 9.330 + 0.589 3 28.00 1.793 + 0.101 3 32.00 0.800 + 0.055 3 48.00 0.123 + 0.072 3 Exam~le 5 Trans~r~l Xanomeline in Acrvlic Adhesive 9.0g Xanomeline free base are dissolved in 91g of an acrylic adhesive solution (solids content 50.0%, cat. number 901-1052, National Starch & Chemical, Zutphen, The Metherlands).The mixture is stirred for at least 0.5 hours and is coated on a 4 mil siliconized polyethylene terephthalate release liner to provide a coated layer of 60 g/m2 (based on dried matter). The wet layer is dried for 30 minutes at room temperature, then for 10 minutes at 50 C. The sample was laminated on a l-mil-backing layer of polyetylene terephthalate.
Test samples of approximately 5 cm2 are punched for in vitro skin permeation experiments on pig ear full thickness skin (Franz type diffusion cell, at 37 C; phosphate buffer pH 4.4 as receptor fluid). A mean (n=3) cumulative permeated amount of 46 ~g Xanomeline was found after 24 hours.
W O 96/23463 PCT~US96/00504 ~XamDle 6 Transdermal Xanomeline in Ac~Ylic ~hecive 14.3g Xanomeline free base are dissolved in 85.7g of an acrylic adhesive solution (solids content 50.0%, cat. number 901-1052, National Starch & Chemical, Zutphen, The Netherlands).
The mixture is stirred for at least 0.5 hours and is coated on a 4 mil siliconized polyethylene terephthalate release liner to provide a coated layer of 60g/m2 (based on dried matter). The wet layer is dried for 30 minutes at room temperature, then for 10 minutes at 50~C. The sample was laminated on a 1-mil-backing layer of polyethylene terephthalate.
Test samples of approximately 5 cm2 are punched for in vitro skin permeation experiments on pig ear full thickness skin (Franz type diffusion cell, at 37~C; phosphate buffer pH 5.5 as receptor fluid). A mean (n=3) cumulative permeated amount of 102 ~g Xanomeline was found after 24 hours.
Exam~le 7 Trans~err-l ~An~m~line in AcrYlic Adhesive 18.0g Xanomeline free base are dissolved in 82g of an acrylic adhesive solution (solids content 50.0%, cat. number 901-1052, National Starch & Chemical, Zutphen, The Netherlands).
The mixture is stirred for at least 0.5 hours and is coated on a 4 mil siliconized polyethylene terephthalate release liner to provide a coated layer of 60 g/m2 (based on dried matter). The wet layer is dried for 30 minutes at room temperature, then for 10 minutes at 50 C. The sample was laminated on a 1-mil-backing layer of polymethacrylic copolymer.
CA 022l07ll l997-07-l6 W 096123463 PCTrUS96/00~04 Test samples of approximately 5 cm2 are punched for in vitro skin permeation experiments on pig ear full thickness skin (Franz type diffusion cell, at 37 C; phosphate buffer pH 5.5 as receptor fluid). A mean (n=2) cumulative permeated amount of 332 ,ug Xanomeline was found after 24 hours.
Examples 5 to 7 illustrate the dependence of xanomeline permeation rate on the concentration o~ the drug.
According to Fick's law, one would expect a linear increase in diffusion (and permeation ) rate with increasing drug concentration. However, the following results based on the examples show an unexpected increase.
Xanomeline Concentration in Permeated after 24 hours dry adhesive matrix (% w/w) ~g/cm2 18 46 (Example 5) 28. 5 102 (Example 6) 36 332 (Example 7) The values had been derived from clear solutions of the drug in the adhesive. Unfortunately, the saturation limit of about 23-28g6 (W/W) in this polymer limits the utilization of this unexpected advantage of highly enriched xanomeline preparations. It is concluded from this unexpected results that an optimum formulation has to contain a slightly subsaturated, saturated or even supersaturated amount of xanomeline for best performance.
Claims (20)
1. A transdermal xanomeline patch formulation comprising as an active ingredient an effective amount of xanomeline, from about 0.1 to 10 parts by weight azone, from about 30 to 69.8 parts ethanol, from about 29 to 50 parts by weight water, from about 0 to 30 parts by weight propylene glycol, and from about 1 to 5 parts by weight gelling agent.
2. A transdermal xanomeline patch formulation of Claim 1, wherein the formulation contains 0 parts by weight propylene glycol.
3. A transdermal xanomeline patch formulation of Claims 1 to 2, wherein the gelling agent is Klucel HF.
4. A transdermal xanomeline patch formulation comprising as an active ingredient an effective amount of xanomeline and from about 88 to 99.8% acrylate adhesive.
5. A transdermal xanomeline patch of Claim 4 wherein the formulation contains from about 80-98% acrylic adhesive.
6. A transdermal xanomeline patch formulation comprising as an active ingredient an effective amount of xanomeline, from about 80 to 97 parts by weight ethanol and from about 2 to 20 parts gelling agent.
7. A transdermal xanomeline patch of Claim 6 wherein the weight of ethanol is from about 85 to 97 parts and gelling agent is about 2 to 15 parts gelling agent.
8. A transdermal xanomeline patch formulation of Claims 6 to 7 wherein the gelling agent is Klucel HF.
9. A xanomeline transdermall using a patch formulation as claimed in any one of Claims 1 to 8 for use in treating a condition associated with modulation of a muscarinic receptor.
10. A formulation of Claim 9 wherein the condition is decreased cognition.
11. A formulation of Claim 9 wherein the condition is Alzheimer's disease.
12. A transdermal patch formulation comprising as an active ingredient an effective amount of xanomeline.
13. A patch formulation as claimed in Claim 12, wherein the xanomeline is intimately distributed in a matrix.
14. A patch formulation as claimed in Claims 12 to 13, wherein the matrix comprises a pressure-sensitive adhesive.
15. A patch formulation as claimed in Claims 12 to 14, wherein the pressure-sensitive adhesive comprises an acrylic adhesive.
16. A patch formulation as claimed in Claims 12 to 14, wherein the matrix comprises a pressure-sensitive adhesive selected from the group consisting of polymers and copolymers of alkyl esters of acrylic acid and methacrylic acid, the alkyl group having from 1 to 18 carbon atoms, athylen-copolymers of vinyl acetate with ethylene or with any of the afore-mentioned acrylic and methacrylic esters, polyvinyl pyrrolidone and copolymers of vinyl pyrrolidone, vinyl acetate or with any of the afore-mentioned acrylic and methacrylic esters.
17. A transdermal patch formulation as claimed in Claims 12 to 16 which additionally contains a permeation enhancer.
18. A transdermal patch formulation as claimed in Claim 17 wherein the enhancer is present in an amount of 0.1 to 10 parts by weight referred to the total amount of the matrix, xanomeline and other constituents, excluding the enhancer, of the matrix.
19. A transdermal patch formulation as claimed in Claims 17 to 18 wherein the permeation enhancer is azone.
20. A transdermal patch formulation as claimed in Claims 12 to 19, wherein the xanomeline is present in an amount of from 0.1 to 35% referred to the total weight of the matrix.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US38047895A | 1995-01-30 | 1995-01-30 | |
| US08/380,478 | 1995-01-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2210711A1 true CA2210711A1 (en) | 1996-08-08 |
Family
ID=23501315
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002210711A Abandoned CA2210711A1 (en) | 1995-01-30 | 1996-01-16 | Transdermal formulation |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US5980933A (en) |
| EP (1) | EP0723781A3 (en) |
| JP (1) | JPH10513181A (en) |
| KR (1) | KR19980701730A (en) |
| AR (1) | AR001790A1 (en) |
| AU (1) | AU709379B2 (en) |
| BR (1) | BR9600216A (en) |
| CA (1) | CA2210711A1 (en) |
| CO (1) | CO4700420A1 (en) |
| CZ (1) | CZ240297A3 (en) |
| EA (1) | EA001083B1 (en) |
| HU (1) | HUP9800832A3 (en) |
| IL (1) | IL116895A (en) |
| NO (1) | NO973471L (en) |
| NZ (1) | NZ301197A (en) |
| PE (1) | PE17397A1 (en) |
| PL (1) | PL321686A1 (en) |
| RO (1) | RO117146B1 (en) |
| TR (1) | TR199700711T1 (en) |
| TW (1) | TW304167B (en) |
| WO (1) | WO1996023463A1 (en) |
| YU (1) | YU5196A (en) |
| ZA (1) | ZA96530B (en) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0821956A1 (en) * | 1996-08-01 | 1998-02-04 | Eli Lilly And Company | Method for treating disruptive behavior disorders |
| US6117890A (en) * | 1996-08-01 | 2000-09-12 | Eli Lilly And Company | Method for treating bipolar disorder |
| US6090829A (en) * | 1996-08-01 | 2000-07-18 | Eli Lilly And Company | Method for treating excessive aggression |
| EP0821954A1 (en) * | 1996-08-01 | 1998-02-04 | Eli Lilly And Company | Method for treating mental retardation |
| US6043258A (en) * | 1996-08-01 | 2000-03-28 | Eli Lilly And Company | Method for treating disruptive behavior disorders with xanomeline |
| US6034108A (en) * | 1997-07-28 | 2000-03-07 | Eli Lilly And Company | Method for treating mental retardation |
| US6193993B1 (en) * | 1998-03-03 | 2001-02-27 | Eisai Co., Ltd. | Suppository containing an antidementia medicament |
| US6528529B1 (en) | 1998-03-31 | 2003-03-04 | Acadia Pharmaceuticals Inc. | Compounds with activity on muscarinic receptors |
| JP5106715B2 (en) * | 1999-09-24 | 2012-12-26 | アルロン・ジャパン株式会社 | Composition for use in a method for releasing L-ascorbic acid, an L-ascorbic acid derivative to the dermal layer of the skin |
| JP3962684B2 (en) * | 2000-11-06 | 2007-08-22 | サムヤン コーポレイション | Transdermal agent having improved water absorption and adhesion |
| EP1928437A2 (en) | 2005-08-26 | 2008-06-11 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
| EP2258357A3 (en) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenesis with acetylcholinesterase inhibitor |
| DE102005050431A1 (en) * | 2005-10-21 | 2007-04-26 | Lts Lohmann Therapie-Systeme Ag | Transdermal therapeutic system for the administration of lipophilic and / or less skin-permeable active ingredients |
| US20070259859A1 (en) * | 2006-05-04 | 2007-11-08 | De Bruin Natasja M W J | Muscarinic agonists to treat impulse control disorders |
| DE102010024105A1 (en) * | 2010-06-17 | 2011-12-22 | Grünenthal GmbH | Transdermal administration of memantine |
| WO2012094360A2 (en) | 2011-01-04 | 2012-07-12 | Gordon Chiu | Biotherapeutics for the treatment of infectious diseases |
| EP3265067A4 (en) | 2015-03-06 | 2018-09-12 | Chase Pharmaceuticals Corporation | Oxybutynin-xanomeline transdermal therapeutic system combinations |
| CA2996717A1 (en) | 2015-09-11 | 2017-03-16 | Chase Pharmaceuticals Corporation | Muscarinic combination and its use for combating hypocholinergic disorders of the central nervous system |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4316893A (en) * | 1975-06-19 | 1982-02-23 | Nelson Research & Development Co. | Vehicle composition containing 1-substituted azacycloalkan-2-ones |
| US5344656A (en) * | 1986-09-12 | 1994-09-06 | Alza Corporation | Subsaturated transdermal therapeutic system having improved release characteristics |
| US4908027A (en) * | 1986-09-12 | 1990-03-13 | Alza Corporation | Subsaturated transdermal therapeutic system having improved release characteristics |
| MY102980A (en) * | 1986-10-31 | 1993-03-31 | Pfizer | Transdermal flux enhancing compositions |
| ATE76584T1 (en) * | 1987-08-28 | 1992-06-15 | Lilly Co Eli | PERMEATION ENHANCING COMPOSITION. |
| IT1233860B (en) * | 1988-02-08 | 1992-04-21 | Isf Spa | PERHYDROAZACYCLA ALCA (1,2-A) IMIDAZOLE BY NOOTROPIC ACTIVITY |
| DE3843239C1 (en) * | 1988-12-22 | 1990-02-22 | Lohmann Therapie Syst Lts | |
| US5043345A (en) * | 1989-02-22 | 1991-08-27 | Novo Nordisk A/S | Piperidine compounds and their preparation and use |
| IE82916B1 (en) * | 1990-11-02 | 2003-06-11 | Elan Corp Plc | Formulations and their use in the treatment of neurological diseases |
| DK198590D0 (en) * | 1990-08-21 | 1990-08-21 | Novo Nordisk As | HETEROCYCLIC COMPOUNDS, THEIR PREPARATION AND USE |
| US5238933A (en) * | 1991-10-28 | 1993-08-24 | Sri International | Skin permeation enhancer compositions |
-
1995
- 1995-02-17 TW TW084101515A patent/TW304167B/zh active
-
1996
- 1996-01-16 PL PL96321686A patent/PL321686A1/en unknown
- 1996-01-16 NZ NZ301197A patent/NZ301197A/en unknown
- 1996-01-16 CZ CZ972402A patent/CZ240297A3/en unknown
- 1996-01-16 HU HU9800832A patent/HUP9800832A3/en unknown
- 1996-01-16 WO PCT/US1996/000504 patent/WO1996023463A1/en not_active Application Discontinuation
- 1996-01-16 AU AU46565/96A patent/AU709379B2/en not_active Ceased
- 1996-01-16 EA EA199700151A patent/EA001083B1/en not_active IP Right Cessation
- 1996-01-16 TR TR97/00711T patent/TR199700711T1/en unknown
- 1996-01-16 KR KR1019970705126A patent/KR19980701730A/en not_active Application Discontinuation
- 1996-01-16 JP JP8523556A patent/JPH10513181A/en active Pending
- 1996-01-16 RO RO97-01416A patent/RO117146B1/en unknown
- 1996-01-16 CA CA002210711A patent/CA2210711A1/en not_active Abandoned
- 1996-01-22 ZA ZA96530A patent/ZA96530B/en unknown
- 1996-01-25 CO CO96003054A patent/CO4700420A1/en unknown
- 1996-01-25 BR BR9600216A patent/BR9600216A/en active Search and Examination
- 1996-01-25 IL IL11689596A patent/IL116895A/en active IP Right Grant
- 1996-01-25 EP EP96300535A patent/EP0723781A3/en not_active Withdrawn
- 1996-01-26 AR AR33519696A patent/AR001790A1/en not_active Application Discontinuation
- 1996-01-29 YU YU5196A patent/YU5196A/en unknown
- 1996-02-02 PE PE1996000080A patent/PE17397A1/en not_active Application Discontinuation
-
1997
- 1997-07-28 NO NO973471A patent/NO973471L/en not_active Application Discontinuation
- 1997-09-29 US US08/942,141 patent/US5980933A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US5980933A (en) | 1999-11-09 |
| EA001083B1 (en) | 2000-10-30 |
| CZ240297A3 (en) | 1998-04-15 |
| IL116895A0 (en) | 1996-05-14 |
| KR19980701730A (en) | 1998-06-25 |
| HUP9800832A2 (en) | 1999-01-28 |
| RO117146B1 (en) | 2001-11-30 |
| EP0723781A3 (en) | 1996-08-07 |
| AU709379B2 (en) | 1999-08-26 |
| AR001790A1 (en) | 1997-12-10 |
| EA199700151A1 (en) | 1997-12-30 |
| CO4700420A1 (en) | 1998-12-29 |
| JPH10513181A (en) | 1998-12-15 |
| IL116895A (en) | 2000-08-31 |
| PE17397A1 (en) | 1997-05-21 |
| WO1996023463A1 (en) | 1996-08-08 |
| NZ301197A (en) | 1999-09-29 |
| PL321686A1 (en) | 1997-12-22 |
| NO973471L (en) | 1997-09-19 |
| NO973471D0 (en) | 1997-07-28 |
| BR9600216A (en) | 1998-01-06 |
| YU5196A (en) | 1998-08-14 |
| AU4656596A (en) | 1996-08-21 |
| ZA96530B (en) | 1997-07-23 |
| TW304167B (en) | 1997-05-01 |
| EP0723781A2 (en) | 1996-07-31 |
| HUP9800832A3 (en) | 2000-07-28 |
| TR199700711T1 (en) | 1998-01-21 |
| MX9705723A (en) | 1997-11-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5980933A (en) | Transdermal formulation of xanomeline | |
| JP4394443B2 (en) | Transdermal preparation | |
| EP2078524A1 (en) | Adhesive skin patch | |
| US5858393A (en) | Transdermal formulation | |
| EP1589973B1 (en) | Formulation and methods for the treatment of thrombocythemia | |
| US5605701A (en) | Transdermal formulation | |
| US20040241240A1 (en) | Percutaneous absorption preparations | |
| JPH10231248A (en) | Percutaneous absorption type preparation containing dihydroetorphine | |
| US20120052112A1 (en) | Risperidone-containing transdermal preparation and adhesive patch using same | |
| EP1787648A1 (en) | Medicinal composition for percutaneous perospirone administration | |
| WO2005041967A1 (en) | Transdermal preparations and method for relieving side effects in pergolide therapy | |
| EP1611882B1 (en) | Adhesive patch | |
| US11291656B2 (en) | Pramipexole transdermal delivery system and uses thereof | |
| MXPA97005723A (en) | Transderm formulation |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |